Canonical Allele Identifier: PA2825295715
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2950820
ClinVar RCV Id: RCV003810130

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Glu1081Asp
CA362683389
NM_001008844.3:c.3243G>C
CA362683390
NM_001008844.3:c.3243G>T